# K001794: Ebi Anterior Cervical Plate System

- Pathway: 510(k) (Special)
- Applicant: Ebi, L.P.
- Decided: Jul 12, 2000 after 28 days
- Product code: KWQ (Appliance, Fixation, Spinal Intervertebral Body)
- Device class: 2
- Regulation: 21 CFR 888.3060
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
13 later devices descend from it; 5 cite it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K173099: Fortis and Hana Anterior Cervical Plate System (2017), 4 descendants of its own
- K222572: FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate System, and BALTEUM™ & BALTEUM-ONE™ Lumbar Plate System (2022), 2 descendants of its own
- K190666: CYGNUS™ Anterior Cervical Plate System (2019), 2 descendants of its own
- K112809: Blue Mountain Cervical Plate (2012), 2 descendants of its own
- K220441: CYGNUS™ MoRe Anterior Cervical Plate System (2022), 1 descendant of its own

Source page: https://510kreport.com/device/K001794
Methodology: https://510kreport.com/methodology